Dear customer, we are very proud to inform you that our company has obtained the MDSAP certification (medical device single audit program) for all countries (Japan, Australie, USA, Canada, Brazil).

Over the years the Teknimed company has evolved and we wanted better reflect its objective and its values.
But our ambition remains constant: Create innovative quality products for the well-being of patients in the world.

Welcome to SOFCOT & MEDICA 2019, November 11-13 in Paris & 18-21 in Düsseldorf.
Join us  booth #F45 & #4H16A. See you soon!!

Teknimed is attending NASS 2019, September 25-28 in Chicago, IL. Come see us at booth # 3625. See you soon!!

Teknimed, 15 new clean rooms at our new production site in L’Union!

Thanks to its new investment in the development of 400 m2 of new clean rooms, Teknimed is increasing its capacity to produce medical devices in the Controlled Atmosphere Zone to 650 m2.

The design and operational qualification (QIQOQP) for the opening of the site has been successfully audited by our notified body the BSI (quality system and microbiological audits).

This new ZAC (Controlled Atmosphere Zone) dedicated to the manufacture of medical devices has been developed and built according to the ISO 14644 standard on the design and implementation of clean rooms and good manufacturing practices (GMP) to meet the requirements. ISO 8, 7 and 5 required and international quality standards GMP.